| Literature DB >> 33429969 |
Diana Cimiotti1, Heidi Budde2, Roua Hassoun2, Kornelia Jaquet2.
Abstract
The sarcomere as the smallest contractile unit is prone to alterations in its functional, structural and associated proteins. Sarcomeric dysfunction leads to heart failure or cardiomyopathies like hypertrophic (HCM) or restrictive cardiomyopathy (RCM) etc. Genetic based RCM, a very rare but severe disease with a high mortality rate, might be induced by mutations in genes of non-sarcomeric, sarcomeric and sarcomere associated proteins. In this review, we discuss the functional effects in correlation to the phenotype and present an integrated model for the development of genetic RCM.Entities:
Keywords: aggregation; calcium; cardiomyopathy; contractile dysfunction; gene expression; pediatric; restrictive cardiomyopathy; sarcomere
Year: 2021 PMID: 33429969 DOI: 10.3390/ijms22020558
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 5.923